JP2009536155A5 - - Google Patents

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Publication number
JP2009536155A5
JP2009536155A5 JP2009505472A JP2009505472A JP2009536155A5 JP 2009536155 A5 JP2009536155 A5 JP 2009536155A5 JP 2009505472 A JP2009505472 A JP 2009505472A JP 2009505472 A JP2009505472 A JP 2009505472A JP 2009536155 A5 JP2009536155 A5 JP 2009536155A5
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JP
Japan
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aliphatic
optionally substituted
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compound
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JP2009505472A
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English (en)
Japanese (ja)
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JP2009536155A (ja
JP5313875B2 (ja
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Priority claimed from PCT/US2007/009006 external-priority patent/WO2007120752A2/en
Publication of JP2009536155A publication Critical patent/JP2009536155A/ja
Publication of JP2009536155A5 publication Critical patent/JP2009536155A5/ja
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Publication of JP5313875B2 publication Critical patent/JP5313875B2/ja
Expired - Fee Related legal-status Critical Current
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JP2009505472A 2006-04-12 2007-04-12 増殖性疾患の処置のためのタンパク質キナーゼplk1の阻害剤として有用な4,5−ジヒドロ−[1,2,4]トリアゾロ[4,3−f]プテリジン Expired - Fee Related JP5313875B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US79132706P 2006-04-12 2006-04-12
US60/791,327 2006-04-12
US83872006P 2006-08-18 2006-08-18
US60/838,720 2006-08-18
PCT/US2007/009006 WO2007120752A2 (en) 2006-04-12 2007-04-12 4, 5-dihydro- [1, 2, 4] triazolo [4, 3-f] pteridines as protein kinase plk1 inhibitors for the treatment of proliferative disorders

Publications (3)

Publication Number Publication Date
JP2009536155A JP2009536155A (ja) 2009-10-08
JP2009536155A5 true JP2009536155A5 (zh) 2010-05-27
JP5313875B2 JP5313875B2 (ja) 2013-10-09

Family

ID=38544378

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009505472A Expired - Fee Related JP5313875B2 (ja) 2006-04-12 2007-04-12 増殖性疾患の処置のためのタンパク質キナーゼplk1の阻害剤として有用な4,5−ジヒドロ−[1,2,4]トリアゾロ[4,3−f]プテリジン

Country Status (17)

Country Link
US (3) US7763629B2 (zh)
EP (1) EP2010542B1 (zh)
JP (1) JP5313875B2 (zh)
KR (1) KR101432316B1 (zh)
AR (1) AR060432A1 (zh)
AT (1) ATE542823T1 (zh)
AU (1) AU2007238690B2 (zh)
CA (1) CA2649324A1 (zh)
ES (1) ES2381212T3 (zh)
HK (1) HK1134486A1 (zh)
IL (1) IL194699A (zh)
MX (1) MX2008013110A (zh)
NO (1) NO20084747L (zh)
NZ (1) NZ571969A (zh)
RU (1) RU2441006C2 (zh)
TW (1) TW200808805A (zh)
WO (1) WO2007120752A2 (zh)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ583061A (en) * 2007-08-15 2012-06-29 Vertex Pharma 4-(9-(3,3-difluorocyclopentyl)-5,7,7-trimethyl-6-oxo-6,7,8,9-tetrahydro-5h-pyrimido[4,5-b[1,4]diazepin-2-ylamino)-3-methoxybenzamide derivatives as inhibitors of the human protein kinases plk1 to plk4 for the treatment of proliferative diseases
MX2010006457A (es) 2007-12-19 2010-07-05 Amgen Inc Compuestos fusionados de piridina, pirimidina y triazina como inhibidores de ciclo celular.
ATE531372T1 (de) 2008-04-07 2011-11-15 Amgen Inc Gem-disubstituierte und spirocyclische aminopyridine/pyrimidine als zellcyclus- inhibitoren
CA2728830A1 (en) * 2008-06-23 2010-01-21 Jean-Damien Charrier Protein kinase inhibitors
WO2010008454A1 (en) * 2008-06-23 2010-01-21 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors
CN102548994A (zh) 2009-09-25 2012-07-04 沃泰克斯药物股份有限公司 用于制备用作蛋白激酶抑制剂的嘧啶衍生物的方法
RU2012116526A (ru) * 2009-09-25 2013-10-27 Вертекс Фармасьютикалз Инкорпорейтед Способы получения производных пиримидина, применимых в качестве ингибиторов протеинкиназы
US8541418B2 (en) 2009-12-23 2013-09-24 Elan Pharmaceutical, Inc. Inhibitors of polo-like kinase
EP2535059A4 (en) * 2010-02-10 2014-03-12 Public Univ Corp Yokohama City USE OF A MSIN3B-BINDING COMPOUND WHICH BINDES SPECIFICLY TO THE SILENCER FACTOR OF NRSF NEURONIC SPECIFICATION
ES2706066T3 (es) 2010-07-02 2019-03-27 Univ Health Network Procedimiento dirigido a enfermedades mutantes con PTEN y composiciones para las mismas
BR112013008526A2 (pt) 2010-10-08 2016-07-12 Elan Pharm Inc inibidores de quinase do tipo polo
US8569331B2 (en) 2010-11-01 2013-10-29 Arqule, Inc. Substituted benzo[f]lmidazo[1,2-d]pyrido[2,3-b][1,4]diazepine compounds
EP2688887B1 (en) 2011-03-23 2015-05-13 Amgen Inc. Fused tricyclic dual inhibitors of cdk 4/6 and flt3
MD4300C1 (ro) * 2012-12-28 2015-03-31 Государственный Университет Молд0 Inhibitor al proliferării celulelor HepG2 în cancerul hepatic în bază de cloro-[2-fenil(piridin-2-il)metanon-4-(3-metoxifenil)tiosemicarbazono]nichel
WO2016183071A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Hetero-tricyclic compounds and their use for the treatment of cancer
WO2017027717A1 (en) 2015-08-12 2017-02-16 Incyte Corporation Bicyclic fused pyrimidine compounds as tam inhibitors
US10053465B2 (en) 2015-08-26 2018-08-21 Incyte Corporation Pyrrolopyrimidine derivatives as TAM inhibitors
SI3436461T1 (sl) 2016-03-28 2024-03-29 Incyte Corporation Pirolotriazinske spojine kot tam-inhibitorji
RS62872B1 (sr) 2017-09-27 2022-02-28 Incyte Corp Soli derivata pirrolotriazina korisne kao tam inhibitori
CN117771250A (zh) 2018-06-29 2024-03-29 因赛特公司 Axl/mer抑制剂的制剂
CN109734809A (zh) * 2019-02-27 2019-05-10 南方科技大学 治疗性的人Plk1蛋白单克隆抗体及其制备方法
JP2023540728A (ja) * 2021-08-10 2023-09-26 オップテラ インコーポレイテッド 新規plk1分解誘導化合物

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA973884B (en) 1996-05-23 1998-11-06 Du Pont Merck Pharma Tetrahydropteridines and pyridylpiperazines for treatment of neurological disorders
US6184226B1 (en) 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
WO2002076985A1 (en) 2001-03-23 2002-10-03 Smithkline Beecham Corporation Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
CA2500727A1 (en) * 2002-10-03 2004-04-15 Targegen, Inc. Vasculostatic agents and methods of use thereof
BRPI0411347A (pt) 2003-06-10 2006-07-11 Pfizer combinações terapêuticas compreendendo inibidores de pde e antagonistas dos receptores de vasopressina para o tratamanento de dismenorréia
GB0315966D0 (en) * 2003-07-08 2003-08-13 Cyclacel Ltd Compounds
GB0400700D0 (en) 2004-01-13 2004-02-18 Pfizer Ltd Compounds useful in therapy
GB0412874D0 (en) 2004-06-09 2004-07-14 Pfizer Ltd Novel pharmaceuticals
DE102004029784A1 (de) * 2004-06-21 2006-01-05 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue 2-Benzylaminodihydropteridinone, Verfahren zur deren Herstellung und deren Verwendung als Arzneimittel

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